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Clinical Data Manager Jobs in Worcester, MA (NOW HIRING)

The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will ...

Director, Data Management

Waltham, MA · On-site

$205K - $230K/yr

Significant experience serving as a Lead Data Manager or equivalent, with direct responsibility for end-to-end clinical data management activities across multiple clinical studies. * Experience ...

Director, Data Management

Waltham, MA · Hybrid

$205K - $230K/yr

Significant experience serving as a Lead Data Manager or equivalent, with direct responsibility for end-to-end clinical data management activities across multiple clinical studies. * Experience ...

NavDx ® , our blood-based DNA test, helps clinicians detect molecular signs of disease recurrence ... Customer Master Data Management - Establish the systems, processes, standards, and governance model ...

NavDx, our blood-based DNA test, helps clinicians detect molecular signs of disease recurrence ... Customer Master Data Management - Establish the systems, processes, standards, and governance model ...

Partner closely with Clinical Operations, Biostatistics, Data Management, Pharmacovigilance, Regulatory Affairs, Translational Medicine, Medical Affairs, Quality, CROs, vendors, and other ...

New

The incumbent applies strong expertise in leading and overseeing set-up and maintenance of Clinical Data Management Systems in addition to providing technical support. This individual supports cross ...

Sr Manager, Data Science

Woonsocket, RI · On-site +1

$140K - $260K/yr

Directs activities of data scientists, providing guidance, mentorship, and performance management ... Collaborates with multiple departments, including clinicians, researchers, and Information ...

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Clinical Data Manager information

See Worcester, MA salary details

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$56

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How much do clinical data manager jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical data manager in Worcester, MA is $56.96, according to ZipRecruiter salary data. Most workers in this role earn between $45.05 and $67.79 per hour, depending on experience, location, and employer.

What does a clinical data manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data manager do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

What are the key skills and qualifications needed to thrive as a clinical data manager?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What are some common challenges clinical data managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

How much do clinical data managers make in the US?

Clinical data managers in the US typically earn between $70,000 and $110,000 annually, with salaries varying based on experience, education, and location. Entry-level positions may start around $60,000, while experienced professionals with specialized skills can earn over $120,000. Certifications in data management and proficiency with electronic data capture systems can also influence salary levels.

What are the most commonly searched types of Clinical Data jobs in Worcester, MA?

The most popular types of Clinical Data jobs in Worcester, MA are:

What are popular job titles related to Clinical Data Manager jobs in Worcester, MA?

For Clinical Data Manager jobs in Worcester, MA, the most frequently searched job titles are:

What cities near Worcester, MA are hiring for Clinical Data Manager jobs?

Cities near Worcester, MA with the most Clinical Data Manager job openings:

Infographic showing various Clinical Data Manager job openings in Worcester, MA as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, and 3% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $118,650 per year, or $57 per hour.

Sr Clinical Data Manager

Clinovo

Waltham, MA • On-site

Contractor

Posted 5 days ago


Job description

Position Overview
A clinical-stage biotechnology company is seeking an experienced Senior Clinical Data Manager Consultant to support its growing clinical development organization.
The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will play a key role in developing and executing clinical data strategies that support high-quality, regulatory-compliant data deliverables.
The ideal candidate will bring significant sponsor-side clinical data management and vendor/CRO oversight experience, along with strong hands-on expertise with Medidata Rave.
This is a senior-level position requiring the ability to independently manage complex data management activities, identify and resolve issues, and effectively collaborate with Clinical Operations, Biostatistics, Statistical Programming, and other cross-functional stakeholders.
Key Responsibilities
  • Lead Clinical Data Management activities across assigned clinical trials from study start-up through database lock.
  • Develop and oversee eCRFs, eCRF completion guidelines, Data Management Plans (DMPs), data review guidelines, edit check specifications, and other study-specific data management documentation.
  • Design, review, and finalize case report forms (CRFs) in collaboration with cross-functional team members.
  • Oversee the implementation and maintenance of study-specific clinical data management systems and processes.
  • Lead and oversee database development, validation, user acceptance testing (UAT), and go-live activities.
  • Develop and execute plans for the processing, review, and cleaning of clinical trial data within established timelines and budgets.
  • Monitor clinical data flow and ensure timely, accurate, and high-quality data availability for analysis.
  • Identify data quality issues and work with internal teams and external partners to drive timely resolution.
  • Provide strong sponsor oversight of CROs, data management vendors, and other external partners responsible for outsourced data management activities.
  • Establish and monitor vendor performance, timelines, deliverables, and data quality expectations.
  • Review clinical protocols and Statistical Analysis Plans (SAPs) to ensure alignment with data collection and management requirements.
  • Ensure clinical data management activities comply with applicable SOPs, ICH-GCP, regulatory requirements, and industry standards.
  • Represent Clinical Data Management in cross-functional study team meetings.
  • Communicate project status, risks, issues, and proposed resolutions to project teams and leadership.
  • Provide recommendations regarding clinical data management processes, systems, and study-specific challenges.
  • Contribute to the continued development and improvement of data management processes, standards, and tools.
  • Monitor study-related data management budgets and evaluate vendor change orders and potential cost overruns.
  • Support audits and regulatory inspections and contribute to corrective and preventive action (CAPA) activities when required.
  • Train and mentor junior team members and promote clinical data management best practices.
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical, Regulatory, and other functional stakeholders.
Required Experience & Qualifications
  • Bachelor's degree in a scientific, clinical, life sciences, or related discipline.
  • Minimum of 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
  • Strong sponsor-side experience, including direct oversight of CROs and external data management vendors.
  • Extensive experience leading Clinical Data Management activities across the full clinical trial lifecycle, from study start-up through database lock.
  • Strong Medidata Rave experience required.
  • Expert knowledge of Electronic Data Capture (EDC) systems; experience with platforms such as Medidata Rave and Veeva.
  • Significant experience with database design, development, validation, and user acceptance testing.
  • Strong understanding of CDISC standards, including CDASH and SDTM.
  • Strong knowledge of ICH-GCP, FDA requirements, and other applicable clinical trial regulations and guidelines.
  • Expert understanding of clinical trial processes, clinical data flow, data review, and data cleaning best practices.
  • Demonstrated experience managing CROs, vendors, and global clinical study teams.
  • Proven ability to lead data management activities for complex and/or global clinical trials.
  • Ability to independently identify and resolve complex data management and technical issues.
  • Strong project management, organizational, and prioritization skills.
  • Excellent written and verbal communication skills.
  • Ability to effectively influence cross-functional stakeholders and senior leadership.
  • Ability to manage multiple priorities and studies within a fast-paced clinical development environment.
Key Candidate Profile
The strongest candidates will combine deep clinical data management expertise with significant sponsor-side oversight experience. Candidates should be comfortable operating independently, managing CRO and vendor deliverables, and serving as the Clinical Data Management subject matter expert within a cross-functional study team.
Medidata Rave expertise and strong sponsor oversight experience are critical requirements for this position.